Diversity and Selectivity of Mycotoxin Fungi Affecting Arachis hypogaea Seed Quality in Western Kenya

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ISSN: 2319-7706 Volume 4 Number 3 (2015) pp. 216-221 http://www.ijcmas.com Original Research Article Diversity and Selectivity of Mycotoxin Fungi Affecting Arachis hypogaea Seed Quality in Western Kenya Javan Omondi Were 1 *, Peres Cherop Ngeywo 1, Julius Onyango Ochuodho 1, Nicholas Kipkemboi Rop 1 and Abigael Adhiambo Owino 1 University of Eldoret, School of Agriculture and Biotechnology, Department of Seed, Crop and Horticultural Sciences, P.O. Box, 1125-30100, Eldoret, Kenya *Corresponding author A B S T R A C T K e y w o r d s Arachis hypogaea, mycotoxin fungi, morphological diversity, variety-pathotype specificity Introduction Decline in ground nut seed quality due to seed-borne fungi contributes to 30-50% potential yield loss in Kenya. Seed infections by mycotoxin fungi not only reduce seed quality but also make nuts unsafe for human consumption. The objective of this study was to assess the morphological diversity and selectivity of mycotoxin producing fungi causing groundnut seed quality deterioration in Western Kenya. The seeds of groundnuts were collected from three markets. Fungal isolation was done using full-strength PDA (39 g/l) under clean airflow and ultraviolet light conditions in the laminar flow. The prepared cultures in petri-dishes were then incubated under continuous white fluorescent at 15-25 o C inside a Gallenkamp incubator. This was repeated till pure isolates were obtained. Morphological diversity assessment and identification was based on mycelial and substrate colour and published references at the plant pathology laboratory, University of Eldoret. Ten morphologically diverse mycotoxin producing fungi were identified to be responsible for low groundnut seed quality in Western Kenya. The most frequently isolated pathotypes were three morphologically diverse strains of Fusarium oxysporum and three strains of Penicillium corylophilum. Two Aspergillus species (A. niger and A. sulphures) and other two unidentified were also isolated. Red Valencia variety of groundnut were the most affected by most mycotoxin fungi but A. niger showed preference to Homa-bay variety while A. sulphures was preferred Red Valencia. The existence of more than one strain of mycotoxin fungi provides the evidence on evolution and differentiation of the fungi alongside the resistant varieties of groundnuts being released by researchers. The gene-for-gene phenomena could be the reason behind the specificity of A. niger and A. sulphures to Homa-bay and Red Valencia varieties respectively. In conclusion, Aspergillus, Fusarium and Penicillium species are responsible for groundnut seed quality deterioration in Western Kenya. Groundnut (Arachis hypogaea) is the sixth most important oilseed crop in the world. It 216 is grown on 26.4 million ha worldwide with a total production of 37.1 million metric t

and an average productivity of 1.4 metric t/ha (FAO, 2003). Over 100 countries worldwide grow groundnut and due to its economic and nutritive value, this crop is a beneficial enterprise for rural farmers in Kenya. The production of groundnut is concentrated in Asia and Africa but in Kenya, its production is mainly concentrated in Western region (Kipkoech et al., 2007). Despite being tolerant to a number of biotic and abiotic stress factors, groundnut responds differently to a number of seed borne pathogens (Burnett and Hunter, 2000; Rasheed et al., 2004). More than 50% yield loss has been reported in Western Kenya due to a number of factors including fungal diseases. Decline in ground nut productivity in Western Kenya has been attributed by a number of factors. This include seed-borne fungal diseases such as Aspergillus flavus with farmers obtaining less than 30-50% of the potential yields (Kipkoech et al., 2007)..A.flavus infects germinating groundnut seed and is associated with grains in storage of which aflatoxins is of utmost concern (Waliyar et al., 2013). This is due to their carcinogens and immunosuppressive effects in both humans and domestic animals (Wu et al., 2011). Most researchers have detected different mycotoxin fungi and their toxin production ability in stored grains, which deteriorate the quality of stored produce (Vedahayagam et al., 1989). However, very little has been done towards detecting the presence and number of mycotoxin producing fungi that affect seed quality in Western Kenya despite the numerous reports of low yields due to seed-borne pathogenic fungi (Nafula, 1997). Due to lack of current and reliable scientific data on mycotoxin producing fungi and their involvement in seed quality deterioration Kenya, the study was set to assess major fungal pathotypes, morphological diversity and pathotype-variety specificity of mycotoxin producing fungi responsible for ground nut seed quality deterioration in Western Kenya. Materials and Methods Study location Infected groundnut seeds of two different varieties (Red Valencia and Homa-bay) were obtained from three markets (Kamkuywa, Kimini and Chwele) in Bungoma County, Western Kenya. Isolation and incubation of mycotoxin fungi Isolation and purification of the mycotoxin fungi from diseased groundnut seeds was done as described by previous researchers (Owino et al., 2013). The groundnut seed samples with symptoms of fungal infection were cut into 1 cm 2 pieces and surfacesterilized in 70 % ethanol for 10 sec and with 1% sodium hypochlorite solution for 30 sec, then rinsed in sterile distilled water for 10 sec three times. Seed pieces were blotted dry and aseptically transferred to freshly prepared potato dextrose agar (PDA Oxoid, 3.9 %) containing streptomycin sulphate (0.39 %) in petri dishes to prevent bacterial growth. Petri dishes were incubated at 15-25 ºC under continuous white fluorescent light inside a Gallenkamp incubator to induce vigorous mycelial growth. Ten days later, a single conidium representing each collection was transferred on freshly prepared potato dextrose agar medium and incubated for two weeks under the same conditions of continuous light and temperature range. 217

Diversity assessment and species identification Data on morphological characteristics including mycelium colour (upper surface) and colour of substrate (under surface), texture and growth of aerial mycelium (luxuriant or scanty) were recorded and used to morphologically assess the diversity of mycotoxin fungi affecting groundnut seed quality. Species identification of the mycotoxin producing fungi was done using plant pathology books and referred journals (Agrios, 2005; Pandey and Sharma, 2010). Result and Discussion Morphological diversity of mycotoxin fungi Ten morphologically diverse species of mycotoxin fungi were observed to lower groundnut seed quality in Western Kenya, Bungoma County. The genus Fusarium and Penicillium was the most frequently isolated across the varieties and regions from which the seeds were sourced. This implies that the two genus of mycotoxin fungi are the major seed-borne pathogens lowering seed quality in the region. For instance, isolates 4, 5 and 6 were identified as the major pathotypes of Fusarium oxysporum with distinct magenta substrate colour turning violet, resembling those identified by Pandey and Sharma, 2010 (Plate 1 and 2). Isolates 1, 3, 7, 8 and 9 were identified to belong to the genus Penicillium and this genus of mycotoxin fungi had highest number of morphologically diverse pathotypes. The higher number of diverse strains indicates the higher frequency at which Penicillium evolves to form new strains and this could be due to its evolutionary advantage of massive gene swapping (Ropars et al., 2014). Isolates 3, 7 and 9 were identified to be strains of Penicillium corylophilum while isolates 1 and 8 were only identified as Penicillium species, showing that the two isolates are still unnamed in terms of species (Plate 1 and 2). The third genus of the mycotoxin fungi isolated in this study was Aspergillus and two isolates were identified as A. Niger (isolate 2) and A. Sulphures (isolate 10). These two species of Aspergillus expressed contrasting morphological difference with A. Niger showing black mycelia and greyish substrate colour. However, A. sulphures showed dirty white mycelial growth with orange substrate colour (Plate 1 and 2). Variety-pathotype specificity of mycotoxin fungi For the variety-pathotype specificity, seed infection by Aspergillus species and Fusarium oxysporum was observed to occur in both Red Valencia and Homa-bay varieties. However, higher incidences of Penicillium corylophilum were observed in Red Valencia variety while Homa-bay variety did not have any incidence (Table 1). Aspergillus niger only infected seeds of Homa-bay variety while A. sulphures showed specificity to Red Valencia variety in terms of the isolates from infected seeds. The observed specificity and selectivity of the pathotypes could be due to the influence of environmental, host plant or pathogenic strain factors (Agrios, 2005). In conclusion, Fusarium oxysporum, Penicillium sp, Penicillium corylophilum, Aspergillus sulphure and Aspergillus niger are the major mycotoxin producing pathogenic fungi affecting groundnut seed quality in Western Kenya but the frequency of infection seems to depend on the 218

pathotype-variety interaction and selectivity of the pathogen. Therefore, there is need for advanced microscopic assessments and genetic diversity studies to give detailed morphogenetic diversity results on the identified mycotoxin producing fungi. Table.1 Mycotoxin fungi affecting groundnut seed quality based on variety and seed source SEED SOURCE VARIETY MYCOTOXIN FUNGUS DIVERSE FUNGI Chwele Aspergillus niger Kamkuywa Homa-bay Fusarium oxyporum 3 Kamkuywa Penicillium sp. Chwele Penicillium sp. Kamkuywa Penicillium corylophilum Kimini Fusarium oxyporum Red valencia Chwele Penicillium corylophilum 4 Kimini Penicillium corylophilum Kamkuywa Aspergillus sulphures Aspergillus sulphures 10 Penicillium corylophilum Penicillium sp Penicillium corylophilum 7 8 9 Fusarium oxysporum Fusarium oxysporum Fusarium oxysporum 6 5 4 Penicillium sp. Aspergillus niger Penicillium corylophilum 1 2 3 Plate 1: Morphological diversity (UPPER SURFACE) of pathogenic fungi infecting Red Valencia Homa-Bay varieties of Arachis hypogea L. in Bungoma county. The isolate numbers correspond to those in plate 2 219

10 7 8 9 6 5 4 1 2 3 Plate 2: Morphological diversity (SUBSTRATE) of pathogenic fungi infecting Red Valencia Homa-Bay varieties of Arachis hypogea L. in Bungoma County. The isolate numbers correspond to those in plate 1 Acknowledgement We would like to sincerely appreciate the tireless support from Jane Yaura (Laboratory technician) who played a major role in the achievement of these results. Other authors whose work aided the success of this work are also appreciated. References Agrios GN. 2005. Plant Pathology. 5th Edition ed. Amsterdam: Elsevier Academic Press, UK. Burnett HL, Hunter BB. 2000. Illustrated Genera of imperfect Fungi, McGraw Hill, New York, 218pp FAO. (2003) The State of Food Insecurity in the World Kipkoech AK, Okiror MA, Okalebo JR, Maritim HK. 2007. Production efficiency and economic potential of different soil fertility management strategies among groundnut farmers of Kenya. Science World Journal 2(1), 15-21. Nafula MM. 1997. Assessment of seedborne pathogens for some improtant 220

crops in Western Kenya. Kenya Agricultural Research Institute, Katumani, Kenya. Owino AA, Ochuodho JO, Were JO. 2013. Morphological diversity of net blotch fungi (Pyrenophora teres) infecting barley (Hordeum vulgare) in barley growing zones of Kenya. Journal of Experimental Biology and Agricultural Sciences 1(6), 474-479. Pandey RR, Sharma G. 2010. Influence of culture media on growth, colony character and sporulation of fungi isolated from decaying vegetable waste. Yeast and Fungal Research 1(8), 157-164. Rasheed S, Dawar S, Ghaffar A, Shaukat SS. 2004. Seed Borne Mycoflora of Groundnut. Pakistan Journal of Botany 36(1), 199-202. Ropars J, Aguileta G, devienne DM, Giraud T. 2014 Massive gene swamping among cheese-making Penicillium fungi. Microbial Cell 1(3), 107-109. Vedahayagam HS, Indulkar A, Rao S. 1989. The occurrence of Aspergillus flavus and aflatoxin in India cotton seed. Journal of Food Science and Technology 23 (2), 73 76. Waliyar F, Osiru M, Sudini HK, Njoroge S. 2013. Aflatoxins: Finding solutions for improved food safety, Reducing Aflatoxins in Groundnuts through Integrated Management and Biocontrol, CGIAR. Wu F, Narrod C, Tiongco M, Liu Y. 2011. The health economics of aflatoxin: Global burden of disease. Aflacontrol, IFPRI, Working paper 4, February, 2011. 221